Microdomain dynamics in single-crystal BaTiO3 during paraelectric-ferroelectric phase transition measured with time-of-flight neutron scattering

A. Pramanick, X. P. Wang, C. Hoffmann, S. O. Diallo, M. R. V. Jørgensen, and X.-L. Wang
Phys. Rev. B 92, 174103 – Published 6 November 2015
PDFHTMLExport Citation

Abstract

Microscopic polar clusters can play an important role in the phase transition of ferroelectric perovskite oxides such as BaTiO3, which have shown coexistence of both displacive and order-disorder dynamics, although their topological and dynamical characteristics are yet to be clarified. Here, we report sharp increases in the widths and intensities of Bragg peaks from a BaTiO3 single crystal, which are measured in situ during heating and cooling within a few degrees of its phase transition temperature TC, using the neutron time-of-flight Laue technique. Most significantly sharper and stronger increases in peak widths and peak intensities were found to occur during cooling compared to that during heating through TC. A closer examination of the Bragg peaks revealed their elongated shapes in both the paraelectric and ferroelectric phases, the analysis of which indicated the presence of microdomains that have correlated 111-type polarization vectors within the {110}-type crystallographic planes. No significant increase in the average size of the microdomains (10nm) near TC could be observed from diffraction measurements, which is also consistent with small changes in the relaxation times for motion of Ti ions measured with quasielastic neutron scattering. The current observations do not indicate that the paraelectric-ferroelectric phase transition in BaTiO3 is primarily caused by an increase in the size of the microscopic polar clusters or critical slowing down of Ti ionic motion. The sharp and strong increases in peak widths and peak intensities during cooling through TC are explained as a result of microstrains that are developed at microdomain interfaces during paraelectric-ferroelectric phase transition.

  • Figure
  • Figure
  • Figure
  • Figure
  • Figure
  • Received 18 August 2015
  • Revised 17 September 2015

DOI:https://doi.org/10.1103/PhysRevB.92.174103

©2015 American Physical Society

Authors & Affiliations

A. Pramanick1,*, X. P. Wang2, C. Hoffmann2, S. O. Diallo2, M. R. V. Jørgensen3, and X.-L. Wang1

  • 1Department of Physics and Materials Science, City University of Hong Kong, Kowloon, Hong Kong SAR
  • 2Chemical and Engineering Materials Division, Oak Ridge National Laboratory, Oak Ridge, Tennessee 37831, USA
  • 3Center for Materials Crystallography, iNANO, and Department of Chemistry, Aarhus University, Aarhus, Denmark

  • *abhijit.pramanick@gmail.com

Article Text (Subscription Required)

Click to Expand

Supplemental Material (Subscription Required)

Click to Expand

References (Subscription Required)

Click to Expand
Issue

Vol. 92, Iss. 17 — 1 November 2015

Reuse & Permissions
Access Options
CHORUS

Article Available via CHORUS

Download Accepted Manuscript
Author publication services for translation and copyediting assistance advertisement

Authorization Required


×
×

Images

×

Sign up to receive regular email alerts from Physical Review B

Log In

Cancel
×

Search


Article Lookup

Paste a citation or DOI

Enter a citation
×